Vertex Pharmaceuticals
GMP Quality Assurance Analytical Sr. Quality Specialist (Contract) 23089
Vertex Pharmaceuticals, Boston, Massachusetts, us, 02298
The GMP QA Analytical Sr. Quality Specialist is recognized as a subject matter expert in the principles and application of quality assurance and compliance in support of the QA Analytical function. The Sr. Quality Specialist supports and executes a wide range of activities related to clinical programs. The senior specialist will focus on change control - events, deviations, and CAPA management. Lab experience - analytical HPLC, data review, and biologics experience is helpful.
Key Duties and Responsibilities:
Provides QA review of the GMP data in support of stability and release of clinical products.
Conducts GMP document review, including procedures, work instructions, specifications, methods, protocols, and method reports.
Supports analytical method validation, verification, and transfer activities for clinical products.
Drafts and enforces Quality Agreements between CMOs/Suppliers and Vertex, as needed.
Supports change control assessment, implementation, and closure; assesses and approves change controls.
Supports quality oversight of root-cause analysis and product impact assessment for deviation and OOS/OOT investigations. Ensures that appropriate CAPA actions are identified. Approves investigations/CAPAs.
Supports generation and maintenance of Quality Metrics to support process improvement activities, as necessary.
Represents QA Analytical on cross-functional teams as an experienced Quality technical resource.
Collaborates with internal and external business partners to resolve quality issues to ensure compliant solutions in support of QA Analytical function.
Identifies and communicates risks and assists with risk mitigation plans as necessary.
Supports internal audit or external audit programs as necessary.
Assists in preparation of audit responses as necessary.
Supports continuous improvement projects; may facilitate improvement efforts.
Knowledge and Skills:
Working knowledge of both the conceptual and practical application of cGMPs in a pharmaceutical setting; in-depth knowledge of global GMP requirements and support of GMP manufacturing and testing.
Working knowledge of basic analytical techniques in a QC setting (examples: HPLC, Dissolution, GC, KF, NMR, XRPD, PSD, Water Activity, Compendial Methods).
Experience in assessing Change Controls.
Experience in leading and managing Event Investigations, Root Cause Analysis (RCA), and monitoring CAPA implementation.
Experience with electronic document management systems (e.g., QDoccs, Trackwise, Veeva).
Experience supporting multiple projects/teams, ability to work in a fast-paced environment and meet quality, accuracy, and timeliness objectives.
Experience working with CMO/CTOs.
Demonstrated ability to work independently to provide QA advice for large, multifaceted projects.
Demonstrated ability to evaluate quality matters and make decisions leveraging technical experience and judgment.
Strong communication skills (written and verbal) and the ability to communicate cross-functionally to a wide variety of audiences.
Education and Experience:
Facilitation/problem-solving/organizational, planning.
Advanced knowledge of GMP regulations and applicability to duties.
Operational QA experience in analytical and/or manufacturing setting, interpretation, and application of cGMPs and applicable guidelines/guidance (examples: ICH, USP).
RCA tools/methodology/technical writing.
Bachelor's degree in a scientific or allied health field (or equivalent degree).
Typically requires 2-4 years of experience, or the equivalent combination of education and experience.
Pay Range:$55-$65/hr
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Key Duties and Responsibilities:
Provides QA review of the GMP data in support of stability and release of clinical products.
Conducts GMP document review, including procedures, work instructions, specifications, methods, protocols, and method reports.
Supports analytical method validation, verification, and transfer activities for clinical products.
Drafts and enforces Quality Agreements between CMOs/Suppliers and Vertex, as needed.
Supports change control assessment, implementation, and closure; assesses and approves change controls.
Supports quality oversight of root-cause analysis and product impact assessment for deviation and OOS/OOT investigations. Ensures that appropriate CAPA actions are identified. Approves investigations/CAPAs.
Supports generation and maintenance of Quality Metrics to support process improvement activities, as necessary.
Represents QA Analytical on cross-functional teams as an experienced Quality technical resource.
Collaborates with internal and external business partners to resolve quality issues to ensure compliant solutions in support of QA Analytical function.
Identifies and communicates risks and assists with risk mitigation plans as necessary.
Supports internal audit or external audit programs as necessary.
Assists in preparation of audit responses as necessary.
Supports continuous improvement projects; may facilitate improvement efforts.
Knowledge and Skills:
Working knowledge of both the conceptual and practical application of cGMPs in a pharmaceutical setting; in-depth knowledge of global GMP requirements and support of GMP manufacturing and testing.
Working knowledge of basic analytical techniques in a QC setting (examples: HPLC, Dissolution, GC, KF, NMR, XRPD, PSD, Water Activity, Compendial Methods).
Experience in assessing Change Controls.
Experience in leading and managing Event Investigations, Root Cause Analysis (RCA), and monitoring CAPA implementation.
Experience with electronic document management systems (e.g., QDoccs, Trackwise, Veeva).
Experience supporting multiple projects/teams, ability to work in a fast-paced environment and meet quality, accuracy, and timeliness objectives.
Experience working with CMO/CTOs.
Demonstrated ability to work independently to provide QA advice for large, multifaceted projects.
Demonstrated ability to evaluate quality matters and make decisions leveraging technical experience and judgment.
Strong communication skills (written and verbal) and the ability to communicate cross-functionally to a wide variety of audiences.
Education and Experience:
Facilitation/problem-solving/organizational, planning.
Advanced knowledge of GMP regulations and applicability to duties.
Operational QA experience in analytical and/or manufacturing setting, interpretation, and application of cGMPs and applicable guidelines/guidance (examples: ICH, USP).
RCA tools/methodology/technical writing.
Bachelor's degree in a scientific or allied health field (or equivalent degree).
Typically requires 2-4 years of experience, or the equivalent combination of education and experience.
Pay Range:$55-$65/hr
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